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Contract Scientific Writer Jobs in Indiana (NOW HIRING)

Veristat

Bachelor's degree required; science-related field preferred. Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting.

Veristat

Bachelor's degree required; science-related field preferred. Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting.

Eurofins Scientific

Bioassay Analyst

Indianapolis, IN · On-site

Company Description Eurofins Scientific is an international life sciences company, providing a ... Contract Research Organisation services. It is one of the market leaders in certain testing and ...

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How much do contract scientific writer jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for contract scientific writer in Indiana is $44.84, according to ZipRecruiter salary data. Most workers in this role earn between $32.02 and $55.82 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a contract scientific writer?

To excel as a Contract Scientific Writer, you need strong scientific knowledge, excellent writing and editing skills, and typically a degree in a science or medical field. Familiarity with reference management software, document collaboration tools, and adherence to style guides like AMA or APA is often required. Attention to detail, time management, and the ability to communicate complex ideas clearly are important soft skills in this role. These competencies are crucial for producing accurate, high-quality scientific documents on deadline and collaborating effectively with researchers and clients.

What are typical challenges that contract scientific writers face in their daily work?

Contract Scientific Writers often juggle multiple projects with tight deadlines, requiring strong time management and organizational skills. Interpreting complex scientific data and ensuring accuracy while translating it into accessible content can be demanding. Additionally, writers must adapt quickly to each client's unique requirements and editorial standards, sometimes working with diverse teams of researchers or subject matter experts. Effective communication and a proactive approach to clarifying expectations with clients help mitigate these challenges and ensure successful project delivery.

What is a contract scientific writer?

A Contract Scientific Writer is a freelance or temporary professional who creates scientific documents, such as research articles, regulatory submissions, clinical study reports, and medical communication materials. They often work with pharmaceutical companies, research institutions, or healthcare organizations to translate complex scientific data into clear, accurate, and accessible content. This role requires strong writing skills, subject matter expertise, and the ability to adhere to industry guidelines. Contract arrangements allow flexibility in workload and project selection, making it an attractive option for experts in scientific communication.

What are the most commonly searched types of Scientific Writer jobs in Indiana? The most popular types of Scientific Writer jobs in Indiana are:
What are popular job titles related to Contract Scientific Writer jobs in Indiana? For Contract Scientific Writer jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Contract Scientific Writer jobs in Indiana look for? The top searched job categories for Contract Scientific Writer jobs in Indiana are:
What cities in Indiana are hiring for Contract Scientific Writer jobs? Cities in Indiana with the most Contract Scientific Writer job openings:
Contract Scientific Writer jobs near you

Deviation Writer

Stark Pharma Solutions Inc

Bloomington, IN • On-site

Contractor

Re-posted 23 hours ago

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates:

https://www.linkedin.com/company/99455976/

Role: Deviation Writer

Location: Indiana (Onsite)

Duration: 6-Month Contract

Position Overview:

We are seeking an experienced Deviation Writer to support Manufacturing Engineering and Quality Operations within a GMP-regulated pharmaceutical or biotechnology environment. This role will be responsible for authoring high-quality deviation investigations, performing root cause analysis, and collaborating with cross-functional teams to ensure timely and compliant resolution of quality events.

The ideal candidate will have strong technical writing skills, experience in deviation management, and the ability to translate complex manufacturing and engineering issues into clear, data-driven investigations.

Key Responsibilities

  • Author, review, and manage deviation investigations within a GMP-regulated environment.
  • Collaborate with Manufacturing, Production Engineering, MS&T, Supply Chain, Quality, and other stakeholders to gather facts and technical information.
  • Conduct and document root cause investigations using structured problem-solving methodologies.
  • Develop robust corrective and preventive action (CAPA) plans based on investigation outcomes.
  • Analyze manufacturing and quality data to support investigation conclusions.
  • Ensure investigations are completed accurately, thoroughly, and within required timelines.
  • Support continuous improvement initiatives related to quality systems and manufacturing processes.
  • Maintain compliance with GMP regulations, internal procedures, and quality standards.
  • Simplify complex technical events into clear, concise, and audit-ready documentation.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Chemistry, Biotechnology, or a related technical discipline.
  • Minimum 3 years of experience in technical writing within a regulated GMP environment.
  • Experience authoring deviation investigations in pharmaceutical, biopharmaceutical, or biotechnology manufacturing.

Strong knowledge of:

  • Root Cause Analysis
  • CAPA Development
  • Deviation Management
  • GMP Regulations
  • Experience using investigation tools such as:
  • Fishbone Analysis
  • 5 Whys
  • Failure Analysis Techniques
  • Familiarity with Electronic Quality Management Systems (eQMS).
  • Strong Microsoft Word and Excel skills.
  • Excellent communication, documentation, and cross-functional collaboration abilities.